Quality Assurance Compliance Manager

JR United Kingdom; Woking; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading company in life sciences is seeking a Quality Assurance Compliance Manager to uphold GxP standards at their Woking site. This leadership role involves ensuring compliance across validation, documentation, and quality processes while fostering a culture of quality in a collaborative environment. The ideal candidate will have strong experience in pharmaceutical QA, especially in GMP contexts, and a knack for stakeholder engagement.

Qualifications

• Strong experience in pharmaceutical QA with a focus on GMP/GDP.
• Background in validation and quality systems.
• Proven expertise in data integrity within regulated environments.

Responsibilities

• Lead QMS compliance activities and continuous improvement.
• Act as data integrity subject matter expert and provide oversight.
• Collaborate with key functions to ensure regulatory compliance.

Skills

Data Integrity

GMP/GDP

Stakeholder Engagement

Quality Oversight

Continuous Improvement

Tools

TrackWise

LIMS

Job description

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Quality Assurance Compliance Manager, Woking

Client: Nexia Life Sciences

Location: Woking, United Kingdom

Job Category: Other

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EU work permit required: Yes

Job Views: 7

Posted: 06.06.2025

Expiry Date: 21.07.2025

Job Description:

Overview:

This leadership role is central to ensuring the site's Quality Management System remains compliant with GxP standards. You’ll act as the site lead for QMS and data integrity, supporting ongoing compliance across validation, documentation, and quality processes. The role sits within the Quality leadership team and plays a key part in building a strong compliance culture across the UK site and affiliate operations.

Key Responsibilities:

• Lead QMS compliance activities across the site, focusing on continuous improvement and adherence to GxP
• Act as the site’s data integrity subject matter expert, advising and educating teams on best practice
• Maintain and develop the site’s validation master plan
• Provide quality oversight on investigations, CAPAs, change controls, and audit readiness
• Collaborate closely with QA, Manufacturing, Validation, and IT functions to ensure systems and processes meet regulatory expectations
• Contribute to the Quality leadership team and support cross-functional quality initiatives

Ideal Experience:

• Strong experience in pharmaceutical QA, with a focus on GMP/GDP
• Background in validation and quality systems (e.g., change control, CAPA, audit prep)
• Proven expertise in data integrity and compliance within a regulated environment
• Confident communicator with solid stakeholder engagement skills
• Familiarity with electronic quality systems (e.g., TrackWise, LIMS) is beneficial